4-Bromo-N-(5-Fluoro-2-Nitrophenyl)Benzenesulfonamide

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Reagent Code: #154002
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CAS Number 1534688-91-9

science Other reagents with same CAS 1534688-91-9

blur_circular Chemical Specifications

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Weight 375.17 g/mol
Formula C₁₂H₈BrFN₂O₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo, fluoro, and nitro groups allows for further functionalization through cross-coupling reactions and reductions, enabling structural diversification. Commonly employed in research settings to design enzyme inhibitors and receptor modulators due to the sulfonamide moiety’s affinity for various biological targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,090.00
inventory 250mg
10-20 days ฿4,990.00
inventory 1g
10-20 days ฿18,930.00

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4-Bromo-N-(5-Fluoro-2-Nitrophenyl)Benzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo, fluoro, and nitro groups allows for further functionalization through cross-coupling reactions and reductions, enabling structural diversification. Commonly employed in research settings to design enzyme

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo, fluoro, and nitro groups allows for further functionalization through cross-coupling reactions and reductions, enabling structural diversification. Commonly employed in research settings to design enzyme inhibitors and receptor modulators due to the sulfonamide moiety’s affinity for various biological targets.

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